SU389660A1 - - Google Patents
Info
- Publication number
- SU389660A1 SU389660A1 SU1695287A SU1695287A SU389660A1 SU 389660 A1 SU389660 A1 SU 389660A1 SU 1695287 A SU1695287 A SU 1695287A SU 1695287 A SU1695287 A SU 1695287A SU 389660 A1 SU389660 A1 SU 389660A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acetoxy
- hydrochloride
- ester
- acid
- dimethylformamide
- Prior art date
Links
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000001766 physiological effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- MPDGHEJMBKOTSU-YKLVYJNSSA-N 18beta-glycyrrhetic acid Chemical compound C([C@H]1C2=CC(=O)[C@H]34)[C@@](C)(C(O)=O)CC[C@]1(C)CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@H](O)C1(C)C MPDGHEJMBKOTSU-YKLVYJNSSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- MPDGHEJMBKOTSU-UHFFFAOYSA-N Glycyrrhetinsaeure Natural products C12C(=O)C=C3C4CC(C)(C(O)=O)CCC4(C)CCC3(C)C1(C)CCC1C2(C)CCC(O)C1(C)C MPDGHEJMBKOTSU-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical class [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- HASGOCLZFTZSTN-UHFFFAOYSA-N cyclohexane;hexane Chemical compound CCCCCC.C1CCCCC1 HASGOCLZFTZSTN-UHFFFAOYSA-N 0.000 description 1
- 229960003720 enoxolone Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19702043479 DE2043479A1 (de) | 1970-09-02 | 1970-09-02 | 3 beta-Acetoxy-11-oxo-noroleanen-(12)-20 beta-carbonsäure-N-methylpiperidol-(4)-ester |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SU389660A1 true SU389660A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| SU389660A3 SU389660A3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1973-07-05 |
Family
ID=5781359
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1695287A SU389660A3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1970-09-02 | 1971-09-02 |
Country Status (20)
-
1970
- 1970-09-02 DE DE19702043479 patent/DE2043479A1/de active Pending
-
1971
- 1971-07-22 FI FI712089A patent/FI48828C/fi active
- 1971-07-22 CH CH1084071A patent/CH556841A/xx not_active IP Right Cessation
- 1971-07-27 NL NL7110335A patent/NL7110335A/xx unknown
- 1971-07-29 ZA ZA715057A patent/ZA715057B/xx unknown
- 1971-07-30 GB GB3595871A patent/GB1301776A/en not_active Expired
- 1971-08-05 IL IL37455A patent/IL37455A/xx unknown
- 1971-08-25 US US00174924A patent/US3758484A/en not_active Expired - Lifetime
- 1971-08-25 FR FR7130847A patent/FR2105177B1/fr not_active Expired
- 1971-08-26 ES ES394538A patent/ES394538A1/es not_active Expired
- 1971-08-27 CS CS6179A patent/CS161132B2/cs unknown
- 1971-08-31 BE BE771984A patent/BE771984A/xx unknown
- 1971-09-01 SE SE7111073A patent/SE385296B/xx unknown
- 1971-09-01 NO NO3261/71A patent/NO133668C/no unknown
- 1971-09-01 AT AT763571A patent/AT306263B/de not_active IP Right Cessation
- 1971-09-01 AU AU32949/71A patent/AU469237B2/en not_active Expired
- 1971-09-01 DK DK430271AA patent/DK127112B/da unknown
- 1971-09-01 BG BG018473A patent/BG19153A3/xx unknown
- 1971-09-02 SU SU1695287A patent/SU389660A3/ru active
- 1971-09-02 CA CA122020A patent/CA934365A/en not_active Expired
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